rs586178

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs586178(C;C)

Make rs586178(C;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

25420739

Gene

RHCE

is a	snp
is	mentioned by
dbSNP	rs586178
dbSNP (classic)	rs586178
ClinGen	rs586178
ebi	rs586178
HLI	rs586178
Exac	rs586178
Gnomad	rs586178
Varsome	rs586178
LitVar	rs586178
Map	rs586178
PheGenI	rs586178
Biobank	rs586178
1000 genomes	rs586178
hgdp	rs586178
ensembl	rs586178
geneview	rs586178
scholar	rs586178
google	rs586178
pharmgkb	rs586178
gwascentral	rs586178
openSNP	rs586178
23andMe	rs586178
SNPshot	rs586178
SNPdbe	rs586178
MSV3d	rs586178
GWAS Ctlg	rs586178

GMAF

0.3421

Max Magnitude

0

OMIM	111700
Desc
Variant	0002
Related	also

ClinVar
Risk	rs586178(A;A) rs586178(C;C)
Alt	rs586178(A;A) rs586178(C;C)
Reference	Rs586178(G;G)
Significance	Non-pathogenic
Disease	RH C/c POLYMORPHISM
Variation	info
Gene	RHCE
CLNDBN	RH C/c POLYMORPHISM
Reversed	0
HGVS	NC_000001.10:g.25747230G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000019283.2,